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Senior Principal Medical Writer - Regulatory - Oncology - Single Sponsor

Syneos Health, Inc.

Mississippi

Remote

USD 114,000 - 211,000

Full time

Today
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Job summary

A leading biopharmaceutical solutions organization is seeking a Senior Principal Medical Writer to develop regulatory documents for submission to global regulatory agencies. The role involves managing medical writing projects and mentoring junior staff in a collaborative environment. A commitment to the culture of development and recognition of individual contributions is essential. The position is remote with a competitive salary range of $114,000 to $210,900.

Benefits

Career development and progression
Supportive and engaged management
Quality-of-life balance

Qualifications

  • Experience with ICH guidelines and global regulatory submissions.
  • Strong communication skills to liaise with various stakeholders.
  • Ability to manage multiple projects under tight deadlines.

Responsibilities

  • Develop regulatory documents for submission to regulatory agencies globally.
  • Manage medical writing projects, including timelines and communications.
  • Participate in cross-functional process improvement initiatives.
  • Mentor junior medical writing staff.

Skills

Regulatory document writing
Project management
Cross-functional collaboration
Mentoring
Job description
Senior Principal Medical Writer - Regulatory - Oncology - Single Sponsor

Updated: October 2, 2025
Location: USA-MS-Remote

Description

Senior Principal Medical Writer - Regulatory - Oncology - Single Sponsor. Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success.

We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do.

Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals.

Why Syneos Health
  • We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.
  • We are committed to our Total Self culture – where you can authentically be yourself.
  • We are continuously building the company we all want to work for and our customers want to work with.
Job Responsibilities
  • Develop regulatory documents for submission to regulatory agencies globally, in accordance with ICH and other global guidelines, standards and processes, and Incyte authoring standards, as applicable.
  • Manage medical writing projects, including developing timelines and communication with cross-functional team members.
  • Participate in cross-functional meetings to provide input regarding medical writing deliverables, timelines, and any process(es) needed for the completion of regulatory documents.
  • Review other documents associated with the assigned project(s), as appropriate.
  • Participate in cross-functional process improvement initiatives.
  • Participate in defining and writing standard operating procedures and best practices for an efficient preparation of quality documents.
  • Manage internal and contract medical writing resources as required to ensure timely completion of assigned projects.
  • Mentor more junior medical writing staff.

We believe in providing an environment and culture in which Our People can thrive, develop and advance. We reward and recognize our people by providing valuable benefits and a quality-of-life balance.

Salary Range: $114,000.00 - $210,900.00

Syneos Health is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, age, religion, marital status, ethnicity, national origin, sex, gender, gender identity, sexual orientation, protected veteran status, disability or any other legally protected status and will not be discriminated against.

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